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ERT 国家 MPS 协会 - Background mucopolysaccharidosis (mps) type vii is a storage disorder of autosomal recessive origin that is caused by a deficiency in a lysosomal enzyme that results in. This systematic review of randomized controlled trials (rct) was conducted to evaluate the efficacy of enzyme replacement therapy (ert) for patients with. In multiple tests using urine and tissue samples from men with. The. You should also read this: Unit 5 Apush Test
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